Disease #06126 (DFNB111 (Deafness, autosomal recessive 111), OMIM:618145)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Global Variome, with Curator vacancy and Johan den Dunnen

Official abbreviation	DFNB111
Name	Deafness, autosomal recessive 111
OMIM ID	618145
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MPZL2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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